M. Araki

发表

Diversity of the damage recognition step in the global genomic nucleotide excision repair in vitro.

K. Sugasawa, F. Hanaoka, S. Iwai, 2001, Mutation research.

Centrosome Protein Centrin 2/Caltractin 1 Is Part of the Xeroderma Pigmentosum Group C Complex That Initiates Global Genome Nucleotide Excision Repair*

K. Sugasawa, F. Hanaoka, C. Masutani, 2001, The Journal of Biological Chemistry.

The carboxy-terminal domain of the XPC protein plays a crucial role in nucleotide excision repair through interactions with transcription factor IIH.

K. Sugasawa, F. Hanaoka, N. Dohmae, 2002, DNA repair.

Reconstitution of damage DNA excision reaction from SV40 minichromosomes with purified nucleotide excision repair proteins.

K. Sugasawa, F. Hanaoka, C. Masutani, 2000, Mutation research.

The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase η

Chikahide Masutani, Shigenori Iwai, Fumio Hanaoka, 1999, Nature.

[Molecular mechanism of nucleotide excision repair in mammalian cells].

F. Hanaoka, C. Masutani, M. Araki, 1999, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.

Identification and characterization of XPC-binding domain of hHR23B

P. J. van der Spek, J. Hoeijmakers, K. Sugasawa, 1997, Molecular and cellular biology.

ATP‐dependent chromatin remodeling facilitates nucleotide excision repair of UV‐induced DNA lesions in synthetic dinucleosomes

Y. Kaneda, F. Hanaoka, S. Iwai, 2001, The EMBO journal.

Xeroderma pigmentosum variant (XP‐V) correcting protein from HeLa cells has a thymine dimer bypass DNA polymerase activity

F. Hanaoka, S. Iwai, C. Masutani, 1999, The EMBO journal.

Xeroderma pigmentosum variant: from a human genetic disorder to a novel DNA polymerase.

T. Eki, F. Hanaoka, S. Iwai, 2000, Cold Spring Harbor symposia on quantitative biology.